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Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Methamphetamine affects gene expression in rat whisker follicles, with key genes linked to addiction.

Chicken feather gene mutation helps understand human hair disorders.

Researchers developed a new method to test hair growth drugs and found that adult cells are best for hair growth, but the method needs improvement as it didn't create mature hair follicles.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

The SOSTDC1 gene is crucial for determining sheep wool type.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

TBX3 gene affects horse coat color, with higher expression in darker areas.

Certain gene variations may protect against skin issues and oxidative stress in women with PCOS.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Innovative methods are reducing animal testing and improving biomedical research.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Melatonin may help with nerve pain, a hepatitis C drug is effective but has side effects, a treatment for mouth sores works but can cause blood issues, ear reconstruction with an implant is safe, HIV transmission from mother to child in Taiwan is now 0% with treatment, certain blood problems are more common in people with a tongue condition, a gene and being overweight are linked to hair loss in some women, a new technique could reduce radiation for lung nodule patients, a hepatitis treatment may lower cancer recurrence after a procedure, and adding extra screening improves tuberculosis detection in patients with lung infections.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Mutations in the AR gene cause hair thinning and loss.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

A new gene, JMJD1C, may affect testosterone levels in men.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Scientists found a gene in mice that causes early hearing loss.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.